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Clinical Trials/NCT03618017
NCT03618017
Completed
Not Applicable

Patient-Centered, Team-Based Continuing Care After Breast Cancer Treatment: The ConnectedCancerCare Pilot Study

University of Michigan Rogel Cancer Center1 site in 1 country66 target enrollmentAugust 8, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Early-stage Breast Cancer
Sponsor
University of Michigan Rogel Cancer Center
Enrollment
66
Locations
1
Primary Endpoint
Number of Breast Cancer Patients Successfully Recruited to Participate in the Study
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

This study is an NCI-funded, randomized control pilot trial to evaluate: (1) the feasibility and acceptability of a web-based, personalized navigation tool (ConnectedCancerCare) and (2) explore whether the tool improves delivery of team-based survivorship care for women who have recently finished primary breast cancer treatment.

Detailed Description

This study is a randomized control pilot trial involving 60 women newly diagnosed with early-stage breast cancer who are finishing primary treatment. Participants will be randomized either to the intervention arm (CCC website that provides information on team-based follow-up care for both cancer surveillance and preventive care) or the control arm (static online survivorship care plan template, adapted from the ASCO breast cancer survivorship template). The feasibility and acceptability of the tool and correlations with patient-reported outcomes will be assessed 3 months following the completion of a baseline survey via an online follow-up survey.

Registry
clinicaltrials.gov
Start Date
August 8, 2018
End Date
August 30, 2019
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Diagnosed with early Stage (0-IIB) breast cancer
  • Must be a patient of a University of Michigan Breast Cancer Oncologist
  • Must be completing primary cancer treatment and transitioning into survivorship
  • Must be able to speak, read and write in English
  • Must have access and the ability to use the internet

Exclusion Criteria

  • Diagnosed with stage III or IV breast cancer
  • Unable to speak, read, and write in English

Outcomes

Primary Outcomes

Number of Breast Cancer Patients Successfully Recruited to Participate in the Study

Time Frame: At baseline survey

We anticipate a response rate of 80% enrollment (n=60). We will assess the number of patients successfully recruited who enroll and complete the baseline survey.

Secondary Outcomes

  • Percentage of Patients That Communicated With PCP About Provider Roles(3 months)
  • Percentage of Patients Reporting a Preference for an Oncologist vs. PCP for Their Continuing Cancer Care Services(3 months)
  • Patient-Reported Satisfaction With Oncologist/PCP Coordination of Care(3 months)
  • Percentage of Patients Scheduling a Primary Care Physician (PCP) Appointment(3 months)
  • Rating the Experience With the CCC Web-based, Survivorship Care Plan(Follow-Up Survey: 3 months)
  • Knowledge About Team-based Survivorship Care(3 months)

Study Sites (1)

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